Test-retest reliability of left and right ventricular systolic function by new and conventional echocardiographic and cardiac magnetic resonance parameters.


Journal

European heart journal. Cardiovascular Imaging
ISSN: 2047-2412
Titre abrégé: Eur Heart J Cardiovasc Imaging
Pays: England
ID NLM: 101573788

Informations de publication

Date de publication:
20 09 2021
Historique:
received: 07 04 2020
accepted: 01 07 2020
pubmed: 15 8 2020
medline: 21 10 2021
entrez: 15 8 2020
Statut: ppublish

Résumé

Reproducible evaluation of left (LV) and right ventricular (RV) function is crucial for clinical decision-making and risk stratification. We evaluated whether speckle-tracking echocardiography (STE) and cardiac magnetic resonance feature-tracking (cMR-FT) global longitudinal (GLS) and circumferential strains allow better test-retest reproducibility of LV and RV systolic function than conventional cMR and echocardiographic parameters. Thirty healthy volunteers and 20 chronic heart failure patients underwent cMR and STE twice on separate days to evaluate test-retest coefficient of variation (CV), intraclass correlation coefficient (ICC) and estimated sample sizes for significant changes in LV and RV function. Among LV parameters, cMR-left ventricular ejection fraction (LVEF) had the highest reproducibility (CV = 6.7%, ICC = 0.98), significantly better than cMR-FT-GLS (CV = 15.1%, ICC = 0.84), global circumferential strains (CV = 11.5%, ICC = 0.94) and echocardiographic LVEF (CV = 11.3%, ICC = 0.93). STE-LV-GLS (CV = 8.9%, ICC = 0.94) had significantly better reproducibility than cMR-FT-LV-GLS. Among RV parameters, STE-RV-GLS (CV = 7.3%, ICC = 0.93) had significantly better CV than cMR-right ventricular ejection fraction (RVEF) (CV = 13%, ICC = 0.82). cMR-FT-RV-GLS (CV = 43%, ICC = 0.39) performed poorly with significantly lower reproducibility than all other RV parameters. Owing to their superior interstudy reproducibility, cMR-LVEF (n = 12), cMR-RVEF (n = 41), STE-LV-GLS and STE-RV-GLS (both n = 14) were the parameters allowing the lowest calculated sample sizes to detect 10% change in LV or RV systolic function. STE-LV-GLS and STE-RV-GLS showed higher test-retest reliability than other echocardiographic measurements of LV and RV function. They also allowed smaller calculated sample sizes, supporting the use of STE-LV and RV-GLS for longitudinal follow-up of LV and RV function.

Identifiants

pubmed: 32793957
pii: 5892442
doi: 10.1093/ehjci/jeaa206
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1157-1167

Informations de copyright

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com.

Auteurs

Laura Houard (L)

Division of Cardiology, Department of Cardiovascular Diseases, Cliniques Universitaires St. LucPôle de Recherche Cardiovasculaire (CARD), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), Av Hippocrate 10/2806, B-1200 Woluwe St. Lambert, Brussels, Belgium.

Sebastian Militaru (S)

Division of Cardiology, Department of Cardiovascular Diseases, Cliniques Universitaires St. LucPôle de Recherche Cardiovasculaire (CARD), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), Av Hippocrate 10/2806, B-1200 Woluwe St. Lambert, Brussels, Belgium.

Kaoru Tanaka (K)

Afdeling Hart en Vaatziekten, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel (VUB), Avenue du Laerbeek 101, B-1090 Brussels, Belgium.

Agnès Pasquet (A)

Division of Cardiology, Department of Cardiovascular Diseases, Cliniques Universitaires St. LucPôle de Recherche Cardiovasculaire (CARD), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), Av Hippocrate 10/2806, B-1200 Woluwe St. Lambert, Brussels, Belgium.

David Vancraeynest (D)

Division of Cardiology, Department of Cardiovascular Diseases, Cliniques Universitaires St. LucPôle de Recherche Cardiovasculaire (CARD), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), Av Hippocrate 10/2806, B-1200 Woluwe St. Lambert, Brussels, Belgium.

Jean-Louis Vanoverschelde (JL)

Division of Cardiology, Department of Cardiovascular Diseases, Cliniques Universitaires St. LucPôle de Recherche Cardiovasculaire (CARD), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), Av Hippocrate 10/2806, B-1200 Woluwe St. Lambert, Brussels, Belgium.

Anne-Catherine Pouleur (AC)

Division of Cardiology, Department of Cardiovascular Diseases, Cliniques Universitaires St. LucPôle de Recherche Cardiovasculaire (CARD), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), Av Hippocrate 10/2806, B-1200 Woluwe St. Lambert, Brussels, Belgium.

Bernhard L Gerber (BL)

Division of Cardiology, Department of Cardiovascular Diseases, Cliniques Universitaires St. LucPôle de Recherche Cardiovasculaire (CARD), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), Av Hippocrate 10/2806, B-1200 Woluwe St. Lambert, Brussels, Belgium.

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Classifications MeSH